Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 19076-57-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 2-formyl-1H-pyrrole-3-carboxylate features a reactive aldehyde group flanked by electron-rich pyrrole and ester functionalities, enabling direct incorporation into heterocyclic scaffolds. This bench-stable reagent facilitates efficient access to functionalized pyrrole derivatives through condensation, cycloaddition, or metal-catalyzed coupling processes under standard conditions.
Ethyl 2-formyl-1H-pyrrole-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrroles and fused polycyclic systems. The ortho-formyl and ester groups provide complementary reactivity for sequential functionalization, including nucleophilic additions, condensations, and transition-metal-catalyzed couplings. Its bench-stable nature and compatibility with common protecting group strategies facilitate streamlined synthetic sequences in medicinal chemistry and materials research.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: